A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400937



Internal ID21058490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84707222..84841610hg38UCSC Ensembl
chr5:84003040..84137428hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38134389
hg19134389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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